4.7 Article

Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder

Journal

TRANSLATIONAL PSYCHIATRY
Volume 11, Issue 1, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1038/s41398-021-01290-1

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Funding

  1. National Institute of Mental Health (NIMH) [MH104255-04]
  2. Brain Research Foundation Fay and Frank Seed Grant
  3. International Obsessive Compulsive Disorder Foundation (IOCDF) Breakthrough Award
  4. One Mind Rising Star Award
  5. National Institute of Health (NIH) Institutional Training Grant [T32NS007433-19]
  6. National Institute of Drug Abuse (NIDA) [T32DA031111]
  7. National Institute of General Medical Sciences of the NIH [T32GM008208]
  8. Achievement Rewards for College Scientists (ARCS) Pittsburgh Chapter Award

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The study sequenced messenger RNA transcripts from the OFC and two striatal regions in OCD subjects and found 904 differentially expressed transcripts compared to unaffected comparison subjects. The research showed that genes involved in synaptic signaling had lower expression in OCD subjects, and there were alterations in cell type fractions in the tissue of OCD subjects.
Obsessive-compulsive disorder (OCD) is a chronic and severe psychiatric disorder for which effective treatment options are limited. Structural and functional neuroimaging studies have consistently implicated the orbitofrontal cortex (OFC) and striatum in the pathophysiology of the disorder. Recent genetic evidence points to involvement of components of the excitatory synapse in the etiology of OCD. However, the transcriptional alterations that could link genetic risk to known structural and functional abnormalities remain mostly unknown. To assess potential transcriptional changes in the OFC and two striatal regions (caudate nucleus and nucleus accumbens) of OCD subjects relative to unaffected comparison subjects, we sequenced messenger RNA transcripts from these brain regions. In a joint analysis of all three regions, 904 transcripts were differentially expressed between 7 OCD versus 8 unaffected comparison subjects. Region-specific analyses highlighted a smaller number of differences, which concentrated in caudate and nucleus accumbens. Pathway analyses of the 904 differentially expressed transcripts showed enrichment for genes involved in synaptic signaling, with these synapse-associated genes displaying lower expression in OCD subjects relative to unaffected comparison subjects. Finally, we estimated that cell type fractions of medium spiny neurons were lower whereas vascular cells and astrocyte fractions were higher in tissue of OCD subjects. Together, these data provide the first unbiased examination of differentially expressed transcripts in both OFC and striatum of OCD subjects. These transcripts encoded synaptic proteins more often than expected by chance, and thus implicate the synapse as a vulnerable molecular compartment for OCD.

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